ConditionPain
Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-60
SponsorCleveland Dental Institute
About this trial
Pain after buffered versus non buffered articaine.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Males and females, age- 18 to 60 yrs.
Medically free.
Need a dental treatment in the upper anterior region.
Disqualifiers
Periodontally affected teeth.
Radiographic bone loss.
Upnormal length of the teeth.
Trial design
Design model
Parallel
Treatments tested in this trial
Buffered articaine
DrugInjecting buffered articaine in maxillary anterior region and evaluate pain response.
Non buffered articaine
DrugInjecting non buffered articaine in maxillary anterior region and evaluate pain response.
Treatment groups
108 Participants
are divided into 2 treatment groupsGroup A: Buffered articaineExperimental treatment 1 intervention
Group B: non buffered articaineActive comparator 1 intervention
Trial outcomes
Primary outcomes
1
Numerical Rate Scale (NRS)
Pain during injection of buffered versus non-buffered articaine local anesthetic will be measured using NRS from 0 to 10, where 0 is no pain and 10 is the most unbearable pain .
Time frame
ImmediateSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov